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Abstract

The concentration of diethylstilbestrol (DES) in the microbial degradation systems was determined using HPLC—UV. Different extraction methods were used in the fungi and bacteria fermentation systems, DES was separated through a Sepax GP-C18 (150 mm×4.60 mm, 5.0 μm), eluted with methanol-water (7︰3, V/V) at 0.7 mL/min, and detected at 242 nm. Results showed that retention time of DES was 7.714 min. Good linearity was obtained with the detection limits of 0.5~50.0 mg/L with a correlation coeffcient of 0.996 3. The average spike recovers of DES for bacteria and fungi fermentation systems were 94.04% and 95.24%, respectively, with RSD of 2.33% and 1.05%, respectively. The limits of detection was not more than 0.30 mg/L. Results showed that the ratios of DES (25 mg/L) degration of four strains could degrade 62.38%, 64.72%, 53.38%, 88.34% , respectively in 5 d. The developed method presented the benefits of simplicity, rapidity, good separation, high accuracy, high precision and good stability.

Publication Date

1-28-2016

First Page

51

Last Page

55

DOI

10.13652/j.issn.1003-5788.2016.01.012

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